
Detail-oriented and proactive clinical research professional with hands-on experience supporting site management, study start-up, and day-to-day trial operations across multiple therapeutic areas. Skilled in coordinating regulatory submissions, maintaining high-quality documentation, and collaborating closely with investigators, site staff, and cross-functional teams to keep studies on track. Recognized for strong communication, problem-solving, and an ability to anticipate operational needs, I bring a consistent focus on compliance, efficiency, and relationship-building to ensure smooth execution across the study lifecycle.